A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6674148



Internal ID10089426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88229685..88229809hg38UCSC Ensembl
Outerchr16:88263291..88263415hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2714977
Supporting Variants
SamplesSSM031
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6674148
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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